US4299967A - Process for producing optically active 2-(2,2-dihalogenovinyl)-cyclopropane-1-carboxylic acids substituted in the 3-position, and derivatives thereof, as well as novel 4-(2,2,2-trihalogenoethyl)-cyclobutane-1-sulfonic acid salts - Google Patents

Process for producing optically active 2-(2,2-dihalogenovinyl)-cyclopropane-1-carboxylic acids substituted in the 3-position, and derivatives thereof, as well as novel 4-(2,2,2-trihalogenoethyl)-cyclobutane-1-sulfonic acid salts Download PDF

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Publication number
US4299967A
US4299967A US06/103,983 US10398379A US4299967A US 4299967 A US4299967 A US 4299967A US 10398379 A US10398379 A US 10398379A US 4299967 A US4299967 A US 4299967A
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United States
Prior art keywords
formula
acid
optically active
methyl
atoms
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Expired - Lifetime
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US06/103,983
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English (en)
Inventor
John G. Dingwall
Hans Greuter
Pierre Martin
Peter Ackermann
Laurenz Gsell
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Novartis Corp
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Ciba Geigy Corp
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Assigned to CIBA-GEIGY CORPORATION reassignment CIBA-GEIGY CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: CIBA-GEIGY AG, A COMPANY OF SWITZERLAND
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides

Definitions

  • the crude product is then dissolved in five times the amount (ml/g) of ethanol/water in a ratio by volume of 1:1, at 60°-70° C.
  • the product obtained after cooling is filtered off and subjected to suction until dry. This crystallisation procedure is carried out a total of 4 times; yield: 60.6 g of fine white needles; melting point 136°-138° C. (decomposition). Further product can be obtained by working up the mother liquors.
  • racemic 2-chloro-3,3-dimethyl-4-(2',2',2'-trichloroethyl)-cyclobutan-1-one used as the starting material can be prepared according to German Offenlegungsschrift No. 2,813,337.
  • racemic 2-chloro-3,3-dimethyl-4-(2',2',2'-tribromoethyl)-cyclobutan-1-one used as the starting material can be prepared as follows:
  • (+)-cyclobutanone (a) 2.0 g (87% of theory) of (+)-cyclobutanone are liberated in the manner described in Example 2 from 3.5 g (5.8 mmols) of the salt obtained according to Example 4.
  • reaction mixture is allowed to warm slowly to room temperature and is stirred for 16 hours at 20° C. and evaporated to dryness under reduced pressure, n-hexane is added to the residue and the organic phase is washed with 1 N hydrochloric acid, saturated sodium bicarbonate solution and sodium chloride solution and dried over MgSO 4 and the solvent is distilled off under reduced pressure. This yields 30 g of a 1:1 mixture of isomers A and B.
  • the cooled melt is digested with ether.
  • the ether phase which has been separated off, is washed with water and filtered through a little silica gel.
  • the organic phase is washed, first twice with, in each case, 500 ml of 2 N hydrochloric acid and then successively with 1,000 ml of 10% potassium carbonate solution and 1,000 ml of saturated sodium bicarbonate solution and three times with 1,000 ml of sodium chloride solution, and dried over magnesium sulfate.
  • the mixture of isomers A and B is resolved by chromatography on a silica gel column using a mixture of 85 parts of petroleum either and 15 parts of diisopropyl ether as the solvent system. First isomer A and then isomer B is obtained. The following specific rotations and refractive indices were measured for the two isomers:
  • Isomer B can also be separated from the resulting mixture of isomers A and B as follows:

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Furan Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
US06/103,983 1978-12-15 1979-12-17 Process for producing optically active 2-(2,2-dihalogenovinyl)-cyclopropane-1-carboxylic acids substituted in the 3-position, and derivatives thereof, as well as novel 4-(2,2,2-trihalogenoethyl)-cyclobutane-1-sulfonic acid salts Expired - Lifetime US4299967A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH12784/78 1978-12-15
CH1278478 1978-12-15

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US06/219,803 Division US4335057A (en) 1978-12-15 1980-12-24 4-(2',2,2'-Trihalogenoethyl)-cyclobutane-1-sulfonic acid salts with optically active bases

Publications (1)

Publication Number Publication Date
US4299967A true US4299967A (en) 1981-11-10

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Family Applications (2)

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US06/103,983 Expired - Lifetime US4299967A (en) 1978-12-15 1979-12-17 Process for producing optically active 2-(2,2-dihalogenovinyl)-cyclopropane-1-carboxylic acids substituted in the 3-position, and derivatives thereof, as well as novel 4-(2,2,2-trihalogenoethyl)-cyclobutane-1-sulfonic acid salts
US06/219,803 Expired - Lifetime US4335057A (en) 1978-12-15 1980-12-24 4-(2',2,2'-Trihalogenoethyl)-cyclobutane-1-sulfonic acid salts with optically active bases

Family Applications After (1)

Application Number Title Priority Date Filing Date
US06/219,803 Expired - Lifetime US4335057A (en) 1978-12-15 1980-12-24 4-(2',2,2'-Trihalogenoethyl)-cyclobutane-1-sulfonic acid salts with optically active bases

Country Status (19)

Country Link
US (2) US4299967A (de)
EP (1) EP0012722B1 (de)
JP (1) JPS5932455B2 (de)
AT (1) ATE468T1 (de)
BR (1) BR7908212A (de)
CA (1) CA1136636A (de)
CS (1) CS214680B2 (de)
DD (1) DD151930A5 (de)
DE (1) DE2961566D1 (de)
DK (1) DK160546C (de)
ES (1) ES8107145A1 (de)
FI (1) FI793891A (de)
GR (1) GR72730B (de)
HU (1) HU184619B (de)
IL (1) IL58963A (de)
MX (1) MX6292E (de)
NO (2) NO150957C (de)
PL (1) PL220431A2 (de)
ZA (1) ZA796855B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4431576A (en) * 1981-02-05 1984-02-14 Roussel Uclaf Perfumant cyclopropane-carboxylic acid derivatives
US5807482A (en) * 1997-10-31 1998-09-15 Uop Llc Chiral stationary phase based on yohimbinic acid
KR19990084855A (ko) * 1998-05-12 1999-12-06 성재갑 시스-퍼메스린산의 광학적 분할방법
US20070129554A1 (en) * 2005-10-24 2007-06-07 Harrington Peter J Alpha functionalization of cyclic, ketalized ketones and products therefrom

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0074856A3 (de) * 1981-09-16 1984-02-01 Glaxo Group Limited Auflösung von racemischen Bicycloheptenonen
US4845272A (en) * 1987-07-10 1989-07-04 Kuraray Co., Ltd. Process for the optical resolution of (±)-cis or (±)-trans-permethric acid
DE19960914A1 (de) * 1998-12-28 2000-06-29 Luk Getriebe Systeme Gmbh Umschlingungsmittel

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028418A (en) * 1975-05-21 1977-06-07 Shell Oil Company Process for the preparation of cyclobutanones
US4064174A (en) * 1976-01-06 1977-12-20 Shell Oil Company Preparation of 2-halocyclobutanones
EP0002206A1 (de) * 1977-11-24 1979-06-13 Ciba-Geigy Ag Halogenierte Buttersäurechloride, Verfahren zu deren Herstellung und ihre Verwendung als Zwischenprodukte zur Herstellung von Schädlingsbekämpfungsmitteln
US4179575A (en) * 1976-09-21 1979-12-18 Roussel Uclaf Polyhalogenated carboxylic acids

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2654062A1 (de) * 1976-08-26 1978-03-23 Bayer Ag Verfahren zur herstellung vinylsubstituierter cyclopropancarbonsaeuren
FI780930A (fi) * 1977-03-31 1978-10-01 Ciba Geigy Ag Foerfarande foer framstaellning av 2-(2'2'2'-trihalogenetyl)-4-halogencyklobutan-1-oner de medelst foerfarandet framstaellda produkterna och deras anvaendning samt de foer deras framstaellning anvaenda mellanprodukterna
US4255351A (en) * 1978-03-14 1981-03-10 Ciba-Geigy Corporation Sulfonic acid esters of 2,2,2-trichloroethylhydroxycyclobutanones

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028418A (en) * 1975-05-21 1977-06-07 Shell Oil Company Process for the preparation of cyclobutanones
US4064174A (en) * 1976-01-06 1977-12-20 Shell Oil Company Preparation of 2-halocyclobutanones
US4179575A (en) * 1976-09-21 1979-12-18 Roussel Uclaf Polyhalogenated carboxylic acids
EP0002206A1 (de) * 1977-11-24 1979-06-13 Ciba-Geigy Ag Halogenierte Buttersäurechloride, Verfahren zu deren Herstellung und ihre Verwendung als Zwischenprodukte zur Herstellung von Schädlingsbekämpfungsmitteln

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Derwent Abst. of Jap. Pat. No. 50-131, 195, and 51-143,647 and 51-36,441. *
Eliel, "Stereochemistry of Carbon Compounds", pp. 49-52 (1962), QD 481, E5. *
Elliott, "Synthetic Pyrethroids", Am. Chem. Soc., Washington, D.C., pp. 2-25 (1977). *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4431576A (en) * 1981-02-05 1984-02-14 Roussel Uclaf Perfumant cyclopropane-carboxylic acid derivatives
US5807482A (en) * 1997-10-31 1998-09-15 Uop Llc Chiral stationary phase based on yohimbinic acid
KR19990084855A (ko) * 1998-05-12 1999-12-06 성재갑 시스-퍼메스린산의 광학적 분할방법
US20070129554A1 (en) * 2005-10-24 2007-06-07 Harrington Peter J Alpha functionalization of cyclic, ketalized ketones and products therefrom

Also Published As

Publication number Publication date
DK160546B (da) 1991-03-25
EP0012722A1 (de) 1980-06-25
ATE468T1 (de) 1981-12-15
DE2961566D1 (en) 1982-02-04
DK533579A (da) 1980-06-16
EP0012722B1 (de) 1981-12-09
BR7908212A (pt) 1980-08-26
JPS5932455B2 (ja) 1984-08-09
CS214680B2 (en) 1982-05-28
ES487505A0 (es) 1980-12-16
ES8107145A1 (es) 1980-12-16
NO150957B (no) 1984-10-08
NO150240C (no) 1984-09-12
JPS5585541A (en) 1980-06-27
DK160546C (da) 1991-09-30
IL58963A (en) 1983-09-30
MX6292E (es) 1985-03-18
PL220431A2 (de) 1980-10-06
HU184619B (en) 1984-09-28
NO150957C (no) 1985-01-16
US4335057A (en) 1982-06-15
IL58963A0 (en) 1980-03-31
ZA796855B (en) 1980-12-31
NO150240B (no) 1984-06-04
NO802540L (no) 1980-06-17
CA1136636A (en) 1982-11-30
GR72730B (de) 1983-12-01
FI793891A (fi) 1980-06-16
NO794102L (no) 1980-06-17
DD151930A5 (de) 1981-11-11

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